T0070907
Based on 45 publication(s) in Google Scholar
T0070907 is a potent PPARγ antagonist with a Ki of 1 nM.
Nur für Forschungszwecke. Wir verkaufen nicht an Patienten.
- Reinheit: 99.94%
- CAS. Nr.: 313516-66-4
- Formel: C12H8ClN3O3
- Molecular Weight:277.66
-
Speicherung:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year
Publications Citing Use of MedChemExpress (MCE) T0070907
More- Signal Transduct Target Ther. 2025 May 9;10(1):150. [Abstract]
- Cancer Cell. 2025 Feb 10;43(2):269-291.e19. [Abstract]
- Nat Commun. 2025 Sep 10;16(1):8215. [Abstract]
- Adv Sci (Weinh). 2025 Nov 11:e08957. [Abstract]
- Theranostics. 2021 Jan 1;11(3):1192-1206. [Abstract]
- EBioMedicine. 2024 Apr:102:105079. [Abstract]
- Proc Natl Acad Sci U S A. 2019 Feb 19;116(8):2996-3005. [Abstract]
- Phytomedicine. 2025 Sep:145:157059. [Abstract]
- Phytomedicine. 2025 Jun 17:145:156986. [Abstract]
- Free Radic Biol Med. 2026 May:248:92-108. [Abstract]
- Arch Pharm Res. 2026 Apr;49(4):554-574. [Abstract]
- Biomed Pharmacother. 2022 Oct:154:113571. [Abstract]
- Stem Cell Res Ther. 2025 Feb 4;16(1):43. [Abstract]
- Stem Cell Res Ther. 2024 May 1;15(1):127. [Abstract]
- Cell Chem Biol. 2023 Sep 21;30(9):1076-1089.e11. [Abstract]
- Aging Cell. 2026 Jun;25(6):e70546. [Abstract]
- Cell Rep. 2025 Apr 16;44(5):115572. [Abstract]
- J Med Chem. 2021 Jan 28;64(2):1018-1036. [Abstract]
- Antioxidants (Basel). 2024 Nov 24;13(12):1446. [Abstract]
- Cell Biosci. 2025 May 14;15(1):59. [Abstract]
- J Agric Food Chem. 2019 Jun 5;67(22):6232-6240. [Abstract]
- Front Immunol. 2019 Nov 14;10:2650. [Abstract]
- Chin Med. 2026 Jan 20;21(1):41. [Abstract]
- Chin Med. 2024 Sep 26;19(1):130. [Abstract]
- Neurobiol Dis. 2018 Sep:117:114-124. [Abstract]
- Food Funct. 2019 Dec 11;10(12):7983-7994. [Abstract]
- Life Sci. 2021 Mar 15:269:119068. [Abstract]
- Int J Mol Sci. 2022 May 1;23(9):5040. [Abstract]
- Int Immunopharmacol. 2026 May 14:182:116849. [Abstract]
- Eur J Pharmacol. 2025 Dec 5:1008:178369. [Abstract]
- Eur J Pharmacol. 2025 Jun 5:996:177445. [Abstract]
- Int Immunopharmacol. 2024 Nov 3;143(Pt 3):113538. [Abstract]
- Int Immunopharmacol. 2023 Oct 10;124(Pt B):111014. [Abstract]
- FEBS J. 2024 Oct;291(20):4581-4601. [Abstract]
- J Mol Med (Berl). 2019 Aug;97(8):1183-1193. [Abstract]
- BMC Complement Med Ther. 2022 Jul 1;22(1):176. [Abstract]
- Front Physiol. 2019 Jun 20:10:798. [Abstract]
- Autoimmunity. 2023 Dec;56(1):2250101. [Abstract]
- Environ Toxicol Chem. 2024 Aug;43(8):1880-1893. [Abstract]
- Exp Physiol. 2020 May;105(5):793-808. [Abstract]
- J Mol Neurosci. 2015 Aug;56(4):848-57. [Abstract]
- In Vitro Cell Dev Biol Anim. 2025 Mar;61(3):288-297. [Abstract]
- Pharmacogn Mag. 205 Jan 27.
- Patent. US20240307497A1.
- Dis Markers. 2022 Oct 3:2022:4158692. [Abstract]
-
RT-PCR
-
WB
-
Flow Cytometry
-
In Vivo Efficacy Study
-
Cell Proliferation/Viability Assay
Biologische Aktivität
|
PPARγ 1 nM (Ki) |
PPARδ 1.8 μM (Ki) |
PPARα 0.85 μM (Ki) |
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| BMDM | IC50 |
0.067 μM
Compound: T007; T0070907
|
Inhibition of osteoclastogenesis in C57BL/6J mouse Bone marrow macrophage cells assessed as inhibition of RANKL-stimulated osteoclast formation measured after 6 days by tartrate-resistant acid phosphatase (TRAP) staining assay
Inhibition of osteoclastogenesis in C57BL/6J mouse Bone marrow macrophage cells assessed as inhibition of RANKL-stimulated osteoclast formation measured after 6 days by tartrate-resistant acid phosphatase (TRAP) staining assay
|
[PMID: 39185622] |
T0070907 (50 μM) pre-treatment impairs repair of IR-induced DNA DSBs in both ME-180 and SiHa cells treated with irradiated (4 Gy). T0070907 (0-50 μM) significantly decreases the levels of DNA-PKcs and RAD51 proteins in ME-180 and SiHa cells[1]. T0070907 (50 μM) treatment reduces the levels of α- and β-tubulin protein in a time-dependent manner, decreases the synthesis of DNA, and prevents the radiation-induced alterations in the cell cycle regulatory proteins of ME180 and SiHa cells[2]. T0070907 (10 μM) has cytotoxicity in an adipocyte-specific and PPARγ-independent manner. T0070907 increases oxidative stress in immature adipocytes[3]. T0070907 (1 μM) blocks the induction of adipogenesis by various treatments of the adipogenic cell line 3T3-L1. T0070907 covalently modifies PPAR on cysteine 313 in helix 3 of human PPAR 2[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
CAS. Nr. 313516-66-4
-
Appearance Solid
-
Molecular Weight 277.66
-
Formel C12H8ClN3O3
-
Color White to light yellow
-
SMILES
ClC1=C(C=C(C=C1)[N+]([O-])=O)C(NC2=CC=NC=C2)=O
-
Versand
Room temperature in continental US; may vary elsewhere.
-
Speicherung
Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year
Publications (45)
-
Journal Impact Factor
-
Most Recent
-
Signal Transduct Target Ther
Myeloid but not hepatocytic CD38 is a key driver for hepatic ischemia/reperfusion injury. [Abstract]2025 May 9;10(1):150. PMID: 40341132 -
Cancer Cell
Adiponectin reduces immune checkpoint inhibitor-induced inflammation without blocking anti-tumor immunity. [Abstract]2025 Feb 10;43(2):269-291.e19. PMID: 39933899 -
Nat Commun
Modulating the PPARγ pathway upregulates NECTIN4 and enhances chimeric antigen receptor (CAR) T cell therapy in bladder cancer. [Abstract]2025 Sep 10;16(1):8215. PMID: 40931013
T0070907 purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Sep 10;16(1):8215. [Abstract]
NECTIN4 mRNA levels in RT112 cells treated with 1 μM Rosiglitazone and T0070907 (T007) for 72 h.
T0070907 purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Sep 10;16(1):8215. [Abstract]
T0070907 (0.5-2.5 μM; 72 h). Western blot for NECTIN4 and HPGD in RT112 cells treated with T0070907, Rosiglitazone, and Pioglitazone at indicated concentrations for 72 h.
T0070907 purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Sep 10;16(1):8215. [Abstract]
NECTIN4 surface staining in RT112 cells treated with 1 μM Rosiglitazone and T0070907 for 72 h.
-
Adv Sci (Weinh)
Mitochondrial CISD1 Modulates Microglial Metabolic Reprogramming to Drive Stress Susceptibility in Mice. [Abstract]2025 Nov 11:e08957. PMID: 41215712
T0070907 purchased from MedChemExpress. Usage Cited in: Adv Sci (Weinh). 2025 Nov 11:e08957. [Abstract]
T0070907 (10 µM; 1 µL per side; microinjected into the mPFC). The social interaction ratio of mice from control, SUS-vehicle, SUS-vehicle-pioglitazone, SUS-T0070907-pioglitazone groups.
-
Theranostics
Suppressing Sart1 to modulate macrophage polarization by siRNA-loaded liposomes: a promising therapeutic strategy for pulmonary fibrosis. [Abstract]2021 Jan 1;11(3):1192-1206. PMID: 33391530 -
EBioMedicine
Peripheral amyloid-β clearance mediates cognitive impairment in non-alcoholic fatty liver disease. [Abstract]2024 Apr:102:105079. PMID: 38507874
T0070907 purchased from MedChemExpress. Usage Cited in: EBioMedicine. 2024 Apr:102:105079. [Abstract]
T0070907 (0-15 μM; 24 h). Viability of HepG2 cells treated with 400 μM PA and indicated concentrations of T0070907 for 24 h.
-
Proc Natl Acad Sci U S A
2019 Feb 19;116(8):2996-3005. PMID: 30718432
T0070907 purchased from MedChemExpress. Usage Cited in: Proc Natl Acad Sci U S A. 2019 Feb 19;116(8):2996-3005. [Abstract]
HT22 cells were pretreated with the indicated inhibitors (CDDO (Bardoxolone, HY-14909); T0070907 (HY-13202); Troglitazone (HY-50935 ); TPCA-1 (HY-10074); JAKi; STAT3i; AV-412 (HY-10346); and MK2206 (HY-10358)) and then treated with T/Z, T/S/Z, T/C/Z for 9 h or Glutamate, Erastin (T: 20 ng/ml; Z: 50 μM; S: 20 nM; C: 1 μg/ml; Glutamate: 50 mM; Erastin 10 μM) for 12 h. Cell viability was measured by CellTiterGlo assay.
-
Phytomedicine
Magnolin Promotes PINK1-Parkin-mediated Mitophagy in Diffuse Large B-cell Lymphoma Cells via PPAR-γ Pathway. [Abstract]2025 Sep:145:157059. PMID: 40680330 -
Phytomedicine
Multi-omics analysis of the active components and mechanisms of Baojin Chenfei formula in silica-induced murine silicosis. [Abstract]2025 Jun 17:145:156986. PMID: 40582209 -
Free Radic Biol Med
Schisandrin B enhances autophagy and random flaps survival through the PPARG-mediated PI3K/AKT/mTOR signaling pathway. [Abstract]2026 May:248:92-108. PMID: 41730481 -
Arch Pharm Res
Tirzepatide mitigates atherosclerosis progression and modulates oxLDL-mediated proatherogenic effects in macrophages: evidence for M1/M2 homeostasis restoration. [Abstract]2026 Apr;49(4):554-574. PMID: 41904760 -
Biomed Pharmacother
Gegen Qinlian decoction ameliorates murine colitis by inhibiting the expansion of Enterobacteriaceae through activating PPAR-γ signaling. [Abstract]2022 Oct:154:113571. PMID: 36007273 -
Stem Cell Res Ther
Intranasal delivery of hMSC-derived supernatant for treatment of ischemic stroke by inhibiting the pro-inflammatory polarization of neutrophils. [Abstract]2025 Feb 4;16(1):43. PMID: 39901221 -
Stem Cell Res Ther
MSCs promote the efferocytosis of large peritoneal macrophages to eliminate ferroptotic monocytes/macrophages in the injured endometria. [Abstract]2024 May 1;15(1):127. PMID: 38693589 -
Cell Chem Biol
Small-molecule MHC-II inducers promote immune detection and anti-cancer immunity via editing cancer metabolism. [Abstract]2023 Sep 21;30(9):1076-1089.e11. PMID: 37236192 -
Aging Cell
Tubular Omega-3 Fatty Acid Receptor FFAR4 Deficiency Aggravated Renal Aging and Chronic Kidney Disease. [Abstract]2026 Jun;25(6):e70546. PMID: 42175992 -
Cell Rep
2025 Apr 16;44(5):115572. PMID: 40249703 -
J Med Chem
Tetrazanbigen Derivatives as Peroxisome Proliferator-Activated Receptor Gamma (PPARγ) Partial Agonists: Design, Synthesis, Structure-Activity Relationship, and Anticancer Activities. [Abstract]2021 Jan 28;64(2):1018-1036. PMID: 33423463 -
Antioxidants (Basel)
Ginsenoside Rg1 Alleviates Blood-Milk Barrier Disruption in Subclinical Bovine Mastitis by Regulating Oxidative Stress-Induced Excessive Autophagy. [Abstract]2024 Nov 24;13(12):1446. PMID: 39765775 -
Cell Biosci
Disrupting lipid homeostasis with CAV2 in OSCC triggers apoptosis, lipolysis, and mitochondrial dysfunction by transcriptional repression of PPARγ. [Abstract]2025 May 14;15(1):59. PMID: 40369665 -
J Agric Food Chem
Combination of Capsaicin and Capsiate Induces Browning in 3T3-L1 White Adipocytes via Activation of the Peroxisome Proliferator-Activated Receptor γ/β3-Adrenergic Receptor Signaling Pathways. [Abstract]2019 Jun 5;67(22):6232-6240. PMID: 31075194 -
Front Immunol
Isovitexin-Mediated Regulation of Microglial Polarization in Lipopolysaccharide-Induced Neuroinflammation via Activation of the CaMKKβ/AMPK-PGC-1α Signaling Axis. [Abstract]2019 Nov 14;10:2650. PMID: 31798583 -
Chin Med
Unraveling the potential mechanisms of Xiaochaihu decoction alleviates metabolic associated fatty liver disease (MAFLD) by integrated transcriptomics, metabolomics, and network pharmacology. [Abstract]2026 Jan 20;21(1):41. PMID: 41559682 -
Chin Med
Qin-Yu-Qing-Chang decoction reshapes colonic metabolism by activating PPAR-γ signaling to inhibit facultative anaerobes against DSS-induced colitis. [Abstract]2024 Sep 26;19(1):130. PMID: 39327592 -
Neurobiol Dis
Bexarotene protects against neurotoxicity partially through a PPARγ-dependent mechanism in mice following traumatic brain injury. [Abstract]2018 Sep:117:114-124. PMID: 29886067 -
Food Funct
Curcumin inhibits cigarette smoke-induced inflammation via modulating the PPARγ-NF-κB signaling pathway. [Abstract]2019 Dec 11;10(12):7983-7994. PMID: 31773117 -
Life Sci
Astragaloside IV protects against podocyte apoptosis by inhibiting oxidative stress via activating PPARγ-Klotho-FoxO1 axis in diabetic nephropathy. [Abstract]2021 Mar 15:269:119068. PMID: 33476631 -
Int J Mol Sci
In Vitro Assays to Identify Metabolism-Disrupting Chemicals with Diabetogenic Activity in a Human Pancreatic β-Cell Model. [Abstract]2022 May 1;23(9):5040. PMID: 35563431 -
Int Immunopharmacol
VPS35 promotes tumor proliferation and migration through the PPARs-ACSL1/4 pathway in lung adenocarcinoma. [Abstract]2026 May 14:182:116849. PMID: 42134293 -
Eur J Pharmacol
Cinobufotalin ameliorates ulcerative colitis by modulating gut microbiota, restoring Th17/Treg balance, and inhibiting MAPK/NF-κB signaling pathways. [Abstract]2025 Dec 5:1008:178369. PMID: 41241337 -
Eur J Pharmacol
The therapeutic potential of Rosiglitazone in modulating scar formation through PPAR-γ pathway. [Abstract]2025 Jun 5:996:177445. PMID: 40054722 -
Int Immunopharmacol
Kaempferol improves depression-like behaviors through shifting microglia polarization and suppressing NLRP3 via tilting the balance of PPARγ and STAT1 signaling. [Abstract]2024 Nov 3;143(Pt 3):113538. PMID: 39492132 -
Int Immunopharmacol
2023 Oct 10;124(Pt B):111014. PMID: 37832237 -
FEBS J
GDH1 exacerbates renal fibrosis by inhibiting the transcriptional activity of peroxisome proliferator-activated receptor gamma. [Abstract]2024 Oct;291(20):4581-4601. PMID: 39136063 -
J Mol Med (Berl)
2019 Aug;97(8):1183-1193. PMID: 31201471 -
BMC Complement Med Ther
Luteolin alleviates inflammation and autophagy of hippocampus induced by cerebral ischemia/reperfusion by activating PPAR gamma in rats. [Abstract]2022 Jul 1;22(1):176. PMID: 35778706 -
Front Physiol
Enterotoxigenic Escherichia coli Interferes FATP4-Dependent Long-Chain Fatty Acid Uptake of Intestinal Epithelial Enterocytes via Phosphorylation of ERK1/2-PPARγ Pathway. [Abstract]2019 Jun 20:10:798. PMID: 31281267 -
Autoimmunity
Proanthocyanidin A2 attenuates the activation of hepatic stellate cells by activating the PPAR-γ signalling pathway. [Abstract]2023 Dec;56(1):2250101. PMID: 37615088 -
Environ Toxicol Chem
Effects of Metabolic Disruption on Lipid Metabolism and Yolk Retention in Zebrafish Embryos. [Abstract]2024 Aug;43(8):1880-1893. PMID: 38860666 -
Exp Physiol
Long non-coding RNA PRRT3-AS1 silencing inhibits prostate cancer cell proliferation and promotes apoptosis and autophagy. [Abstract]2020 May;105(5):793-808. PMID: 32086850 -
J Mol Neurosci
Lipoxin A4 Activates Nrf2 Pathway and Ameliorates Cell Damage in Cultured Cortical Astrocytes Exposed to Oxygen-Glucose Deprivation/Reperfusion Insults. [Abstract]2015 Aug;56(4):848-57. PMID: 25702137 -
In Vitro Cell Dev Biol Anim
5-Azacytidine inhibits endoplasmic reticulum stress and apoptosis of nucleus pulposus cells by preserving PPARγ via promoter demethylation. [Abstract]2025 Mar;61(3):288-297. PMID: 40102314 -
-
-
Dis Markers
Rosiglitazone Alleviates Contrast-Induced Acute Kidney Injury in Rats via the PPAR γ/NLRP3 Signaling Pathway. [Abstract]2022 Oct 3:2022:4158692. PMID: 36225198
Lösungsmittel & Löslichkeit
DMSO : 62.5 mg/mL (225.10 mM; ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
H2O : < 0.1 mg/mL (insoluble)
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 1 mg/mL (3.60 mM); Clear solution
This protocol yields a clear solution of ≥ 1 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (10.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 1 mg/mL (3.60 mM); Clear solution
This protocol yields a clear solution of ≥ 1 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (10.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
Please enter the basic information of animal experiments:
-
-
-
-
Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
-
%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
-
%+
-
+%Tween-80 + +
-
%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL.
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Protokoll
To determine the binding affinity of T0070907 to the PPARs, scintillation proximity assay (SPA) is performed with the following modifications. A 90 μL reaction contains SPA buffer (10 mM K2HPO4, 10 mM KH2PO4, 2 mM EDTA, 50 mM NaCl, 1 mM dithiothreitol, 2 mM CHAPS, 10% (v/v) glycerol, pH 7.1), 50 ng of GST-PPAR (or 150 ng of GST-PPAR), 5 nM 3H-labeled radioligands, and 5 μL of T0070907 in Me2SO. After incubation for 1 h at room temperature, 10 μL of polylysine-coated SPA beads (at 20 mg/mL in SPA buffer) are added, and the mixture is incubated for 1 h before reading in Packard Topcount. [3H]Rosiglitazone is used for PPAR, and [3H]GW2433 is used for PPAR and PPAR.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Reinheit & Dokumentation
-
Data Sheet (277 KB)
-
SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
-
Handling Instructions (2659 KB)
Verweise
[1]. An Z, et al. T0070907 inhibits repair of radiation-induced DNA damage by targeting RAD51. Toxicol In Vitro. 2016 Dec;37:1-8 [Content Brief]
[2]. An Z, et al. T0070907, a PPAR γ inhibitor, induced G2/M arrest enhances the effect of radiation in human cervical cancer cells through mitotic catastrophe. Reprod Sci. 2014 Nov;21(11):1352-61. [Content Brief]
[3]. Kawahara A, et al. Peroxisome proliferator-activated receptor γ (PPARγ)-independent specific cytotoxicity against immature adipocytes induced by PPARγ antagonist T0070907. Biol Pharm Bull. 2013;36(9):1428-34 [Content Brief]
[4]. Lee G, et al. T0070907, a selective ligand for peroxisome proliferator-activated receptor gamma, functions as an antagonist of biochemical and cellular activities. J Biol Chem. 2002 May 31;277(22):19649-57. Epub 2002 Mar 4 [Content Brief]
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 3.6015 mL | 18.0076 mL | 36.0153 mL | 90.0382 mL |
| 5 mM | 0.7203 mL | 3.6015 mL | 7.2031 mL | 18.0076 mL | |
| 10 mM | 0.3602 mL | 1.8008 mL | 3.6015 mL | 9.0038 mL | |
| 15 mM | 0.2401 mL | 1.2005 mL | 2.4010 mL | 6.0025 mL | |
| 20 mM | 0.1801 mL | 0.9004 mL | 1.8008 mL | 4.5019 mL | |
| 25 mM | 0.1441 mL | 0.7203 mL | 1.4406 mL | 3.6015 mL | |
| 30 mM | 0.1201 mL | 0.6003 mL | 1.2005 mL | 3.0013 mL | |
| 40 mM | 0.0900 mL | 0.4502 mL | 0.9004 mL | 2.2510 mL | |
| 50 mM | 0.0720 mL | 0.3602 mL | 0.7203 mL | 1.8008 mL | |
| 60 mM | 0.0600 mL | 0.3001 mL | 0.6003 mL | 1.5006 mL | |
| 80 mM | 0.0450 mL | 0.2251 mL | 0.4502 mL | 1.1255 mL | |
| 100 mM | 0.0360 mL | 0.1801 mL | 0.3602 mL | 0.9004 mL |